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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337182Generated: October 26, 2026

Pyridine → 3-Acetoxycyclohexene

https://huagongshe.com/reaction/337182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Cyclohexen-1-OLHCID 13198—
Product3-AcetoxycyclohexeneHCID 1111614894%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-cyclohexen-1-ol (16) (45.5 mmol, 5.02 mL) in pyridine (0.27 mol, 22 mL) at 0° C., acetic anhydride was added dropwise and the reaction mixture was stirred at 0° C. for ½ h. The ice bath was removed, and the mixture was stirred at room temperature overnight. The mixture was diluted with EtOAc, washed with HCl (1 N), saturated NaHCO3, brine, and concentrated in vacuo to give 6 g (94%) of the crude product 17 which was used in the next step without further purification. TLC with 20% EtOAc/Hexane, stained with 5% H2SO4/EtOH, Rf for (16): 0.4, Rf for (17): 0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889719B2
Source datasetuspto-grants-2014_11
ORD IDord-9b69b1c899954ecc88c475798102edee
Source noteuspto-grants-2014_11